Pharma Quality Control Professional
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I provide professional Quality Control documentation review and GMP compliance support with 9+ years of experience in the pharmaceutical industry. I can assist with: • SOP drafting and review • Change control documentation • Deviation documentation • OOS/OOT review • Audit preparation (EU audit exposure) • QC data review • AMV(Analytical Method Validation) I ensure accuracy, regulatory compliance, and timely delivery. Best for pharma companies, consultants, and regulatory teams needing structured documentation support.
am a Quality Control professional with over 9 years of experience in pharmaceutical industry. I specialize in documentation review, change control, deviation handling, and regulatory compliance. I have hands-on experience with HPLC, IR Spectroscopy, and analytical instruments. I have successfully faced EU audits and ensured full compliance with GMP guidelines. I am detail-oriented, process-driven, and committed to delivering high-quality work with accuracy and timeliness. I can help with: • QC documentation review • SOP drafting & review • Change control support • Deviation management • Audit preparation • Data entry & compliance documentation Available for remote support and consulting projects.